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[ CAS No. 49860-76-6 ] {[proInfo.proName]}

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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
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3d Animation Molecule Structure of 49860-76-6
Chemical Structure| 49860-76-6
Chemical Structure| 49860-76-6
Structure of 49860-76-6 * Storage: {[proInfo.prStorage]}
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Product Details of [ 49860-76-6 ]

CAS No. :49860-76-6 MDL No. :MFCD28361149
Formula : C7H16N2 Boiling Point : -
Linear Structure Formula :- InChI Key :TXIOGJHPPVXTOY-UHFFFAOYSA-N
M.W : 128.22 Pubchem ID :12229105
Synonyms :

Calculated chemistry of [ 49860-76-6 ]

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 47.27
TPSA : 6.48 Ų

Pharmacokinetics

GI absorption : Low
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -7.1 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.26
Log Po/w (XLOGP3) : -0.03
Log Po/w (WLOGP) : -0.51
Log Po/w (MLOGP) : 0.57
Log Po/w (SILICOS-IT) : 0.67
Consensus Log Po/w : 0.59

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -0.55
Solubility : 36.1 mg/ml ; 0.282 mol/l
Class : Very soluble
Log S (Ali) : 0.34
Solubility : 283.0 mg/ml ; 2.21 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : -0.8
Solubility : 20.2 mg/ml ; 0.158 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.29

Safety of [ 49860-76-6 ]

Signal Word:Danger Class:3,6.1
Precautionary Statements:P210-P233-P240-P241+P242+P243-P264-P280-P302+P352+P312+P361+P364-P305+P351+P338+P337+P313-P312-P370+P378-P403+P235-P405-P501 UN#:1992
Hazard Statements:H226-H311-H315-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 49860-76-6 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 49860-76-6 ]

[ 49860-76-6 ] Synthesis Path-Downstream   1~6

YieldReaction ConditionsOperation in experiment
99% With (CuAl)O(x); hydrogen; In tetrahydrofuran; at 120℃; under 3750.38 Torr; for 9.0h; General procedure: The catalyst A 50 mg prepared in Example 1 was weighed,93 mg (1 mmol) of aniline,36 mg (1.2 mmol) of paraformaldehyde and 3 mL of tetrahydrofuran,Were successively added to 100 mL of a reactor equipped with a magnetic stirrer.Sealed with H2 gas replacement system in the air 3 times,Then filled with 0.5MPa H2.The temperature was raised to 120 C and held for 9 hours.The reaction was stopped and cooled to room temperature,Using the centrifuge (Shanghai Anting Science Instrument Factory) to 8000 r / min centrifugal 5 minutes,The catalyst was recovered by recovering from the reaction mixture.Using Agilent 7890A (30m × 0.25mm × 0.33mum capillary column, hydrogen flame ion detector)The reaction mixture was quantitatively analyzed by gas chromatograph.Other by-products were qualitatively analyzed using an Agilent 6890/5973 Gas Chromatography-Mass Spectrometer (equipped with NIST Mass Spectral Database ChemStation, 30m × 0.25mm × 0.33mum Capillary Column).The reaction product is N-methylaniline,
92% With hydrogen; In hexane; at 160℃; under 52505.3 Torr; for 24.0h;Autoclave; General procedure: The procedures were same as that in Example 19. Ina 100 mE reaction autoclave with magnetic stirring, 50 mgCatalyst A was used. The reaction medium was 2 mE n-hexane. 1 mmol starting material was added respectively. After being sealed, the inside of the autoclave was replaced by carbon dioxide gas for three times. Then carbon dioxide gas and hydrogen gas were charged, wherein the starting material, the pressure of the autoclave afier charging carbon dioxide and hydrogen gas (02 and H2? respectively), reaction temperature, reaction time and target products (qualitative analysis and detection were similar to those in Example 46) were shown in Table 2 below, respectively. After stopping the reaction and cooling to RT, the reaction mixture was subjected to a quantitative analysis withAgilent 7890A gas-mass chromatograph (30 mx0.25 mmx0.33 tm capillary column, with a hydrogen flame ionization detector). The target products were obtained by the conventional separation and purification methods well known in the art, such as rectification.The yields ofthe target products were shown in Table 2 below.
  • 4
  • 3-(4-trifluoromethanesulfonyloxyphenyl)-5,5'-dimethoxyspiro[indene-1,1'-indan] [ No CAS ]
  • [ 49860-76-6 ]
  • [ 678996-51-5 ]
YieldReaction ConditionsOperation in experiment
With potassium dihydrogenphosphate; johnphos;palladium diacetate; In 1,4-dioxane; at 80℃; for 20.0h; 3-[4-(Trifluoromethanesulfonyloxy)phenyl]-5,5'-dimethoxyspiro[indene-1,1'-indan] (0.5 g) obtained in Example N, potassium phosphate (0.3 g), 1-ethylpiperazine (0.15 mL), palladium acetate (16 mg) and 2-(di-tert-butylphosphino)biphenyl (45 mg) were placed in a flask, and the air was purged with argon. Anhydrous 1,4-dioxane (4 mL) was added thereto and the mixture was heated at 80C for 20 hr. After allowing to cool, the reaction mixture was filtered and washed with ethyl acetate. The filtrate and the washing solution was combined and the mixture was concentrated under reduced pressure. The residue was subjected to basic silica gel column chromatography (ethyl acetate/hexane) to give the title compound (0.28 g) as an oil.The above-mentioned oil (0.28 g), diphenylphosphine (0.89 g) and butyl lithium (3 mL) were reacted and treated in the same manner as in Example 1 to give the title compound (0.22 g).
  • 5
  • [ 5308-25-8 ]
  • [ 201230-82-2 ]
  • [ 49860-76-6 ]
  • 6
  • [ 5308-25-8 ]
  • [ 124-38-9 ]
  • [ 49860-76-6 ]
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